UDI device identifier
RENASYS F MEDIUM W/SOFT PORT 66020795
UDI device identifier 00040565127170 · SMITH & NEPHEW MEDICAL LIMITED
Key facts
| Primary DI | 00040565127170 |
|---|---|
| Brand name | RENASYS F MEDIUM W/SOFT PORT |
| Version or model | 66020795 |
| Catalog number | 66020795 |
| Company | SMITH & NEPHEW MEDICAL LIMITED |
| DUNS number | 216344051 |
| Product code | OMP |
| GMDN term | Wound dressing kit, medicated |
| Premarket submission | K142979 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Apr 24, 2020 |
| Version date | Sep 7, 2023 |
| Description | RENASYS-F Foam Dressing Kit with Soft Port Medium |
At a glance
- 1–9 MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 100–999 GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: